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The Effect of Fatigue on CPR

NCT06280118 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 84

Last updated 2024-02-28

No results posted yet for this study

Summary

Background: This study, in contrast to the previous studies, generated a scenario of fatigue in an earthquake scenario and aimed to measure the effect of fatigue on the quality of cardiopulmonary resuscitation (CPR) performed by paramedics in a debris course.

Methods: The study was designed as a randomized controlled trial. The sample, consisting of 84 paramedic students, was randomly assigned as 42 control and 42 experimental groups. Fatigue was created in the participants by rehearsing the process of removing and transporting earthquake victims from the rubble through the prepared track. A personal information form and a CPR measurement form were used to obtain the data. The simulator was used to evaluate the accuracy of CPR. The collected data were analysed with the statistical program.

Conditions

  • Resuscitation

Interventions

OTHER

Fatigue

Fatigue was created in the participants by rehearsing the process of removing and transporting earthquake victims from the rubble through the prepared track.

Sponsors & Collaborators

  • Artvin Coruh University

    lead OTHER

Principal Investigators

  • Oğuzhan Tiryaki, Expert Nursing · Artvin State Hospital

  • Elif Tiryaki, Lecturer · Artvin Çoruh University

  • Suat Çelik, Lecturer · Artvin Çoruh University

  • Hüseyin Bora Saçar, Lecturer · Artvin Çoruh University

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
24 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-04-20
Primary Completion
2023-06-20
Completion
2023-10-25

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06280118 on ClinicalTrials.gov